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Complement regulator-acquiring surface protein 1 of Borrelia burgdorferi binds to human bone morphogenic protein 2, several extracellular matrix proteins, and plasminogen

Lyme disease-causing Borrelia burgdorferi spirochetes express up to 5 complement regulator-acquiring surface proteins (CRASPs). To better define how CRASP-1 contributes to infection, we aimed to identify novel CRASP-1-binding host proteins. Here, we identified a number of novel human CRASP-1-binding...

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Bibliographische Detailangaben
Hauptverfasser: Hallström, Teresia (VerfasserIn) , Haupt, Katrin (VerfasserIn) , Kraiczy, Peter (VerfasserIn) , Hortschansky, Peter (VerfasserIn) , Wallich, Reinhard (VerfasserIn) , Skerka, Christine (VerfasserIn) , Zipfel, Peter F. (VerfasserIn)
Dokumenttyp: Article (Journal)
Sprache:Englisch
Veröffentlicht: 21 June 2010
In: The journal of infectious diseases
Year: 2010, Jahrgang: 202, Heft: 3, Pages: 490-498
ISSN:1537-6613
DOI:10.1086/653825
Online-Zugang:Verlag, lizenzpflichtig, Volltext: https://dx.doi.org/10.1086/653825
Verlag, lizenzpflichtig, Volltext: https://academic.oup.com/jid/article/202/3/490/831946
Volltext
Verfasserangaben:Teresia Hallström, Katrin Haupt, Peter Kraiczy, Peter Hortschansky, Reinhard Wallich, Christine Skerka and Peter F. Zipfel
Beschreibung
Zusammenfassung:Lyme disease-causing Borrelia burgdorferi spirochetes express up to 5 complement regulator-acquiring surface proteins (CRASPs). To better define how CRASP-1 contributes to infection, we aimed to identify novel CRASP-1-binding host proteins. Here, we identified a number of novel human CRASP-1-binding proteins, including bone morphogenic protein 2, collagen I, collagen III, collagen IV, fibronectin, laminin, and plasminogen. The plasminogen-binding regions were located in 2 separate regions of CRASP-1. Our results demonstrated that plasminogen-bound CRASP-1 can be converted to plasmin by the urokinase-type plasminogen activator and that proteolytically active plasmin cleaves the synthetic chromogenic substrate S-2251 and the natural substrate fibrinogen. In conclusion, CRASP-1 is a multifunctional protein of B. burgdorferi that binds to several human extracellular matrix proteins and plasminogen. These interactions may contribute to adhesion, bacterial colonization, and organ tropism and may allow dissemination of B. burgdorferi in the host.
Beschreibung:Gesehen am 07.06.2021
Beschreibung:Online Resource
ISSN:1537-6613
DOI:10.1086/653825

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